Pilot Study of Psilocybin-Assisted Therapy for Demoralization in Patients Receiving Hospice Care

NCT04950608 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2026-02-17

Study results available
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Summary

The overall objective of this study is to develop and pilot test a novel regimen of psilocybin-assisted psychotherapy for demoralization in patients receiving hospice care.

-The name of the study drug involved in this study is Psilocybin

Conditions

  • Hospice
  • Psilocybin
  • Demoralization
  • Terminal Illness
  • Cancer-related Problem/Condition
  • Psychotherapy
  • Terminal Cancer
  • Cancer Terminal

Interventions

DRUG

Psilocybin

Oral, single administration, dosage 25 mg orally

BEHAVIORAL

Psychotherapy

The treatment regimen consists of a single administration of psilocybin orally combined with a supportive psychotherapy including 2 preparation sessions and 2 integration sessions

Sponsors & Collaborators

  • Oppenheimer Family Psychosocial Oncology and Palliative Care Research Grants

    collaborator UNKNOWN
  • Usona Institute

    collaborator OTHER
  • Carey and Claudia Turnbull Family Foundation

    collaborator UNKNOWN
  • Heffter Research Institute

    collaborator OTHER
  • George Sarlo Foundation

    collaborator UNKNOWN
  • RiverStyx Foundation

    collaborator OTHER
  • Council on Spiritual Practices Fund at the San Francisco Foundation

    collaborator UNKNOWN
  • Nikean Foundation

    collaborator UNKNOWN
  • Jack Smith

    collaborator UNKNOWN
  • Yvan Beaussant, MD, MSci

    lead OTHER

Principal Investigators

  • Yvan Beaussant, MD · Dana-Farber Cancer Institute

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-09
Primary Completion
2024-07-27
Completion
2025-12-31
FDA Drug
Yes

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04950608 on ClinicalTrials.gov